Postgraduation School in Radiodiagnostics, University of Milan, Milan, Italy.
Department of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Eur Radiol. 2024 Apr;34(4):2699-2710. doi: 10.1007/s00330-023-10260-8. Epub 2023 Oct 12.
MRI-derived extracellular volume (ECV) allows characterization of myocardial changes before the onset of overt pathology, which may be caused by cancer therapy cardiotoxicity. Our purpose was to review studies exploring the role of MRI-derived ECV as an early cardiotoxicity biomarker to guide timely intervention.
In April 2022, we performed a systematic search on EMBASE and PubMed for articles on MRI-derived ECV as a biomarker of cancer therapy cardiotoxicity. Two blinded researchers screened the retrieved articles, including those reporting ECV values at least 3 months from cardiotoxic treatment. Data extraction was performed for each article, including clinical and technical data, and ECV values. Pooled ECV was calculated using the random effects model and compared among different treatment regimens and among those who did or did not experience overt cardiac dysfunction. Meta-regression analyses were conducted to appraise which clinical or technical variables yielded a significant impact on ECV.
Overall, 19 studies were included. Study populations ranged from 9 to 236 patients, for a total of 1123 individuals, with an average age ranging from 12.5 to 74 years. Most studies included patients with breast or esophageal cancer, treated with anthracyclines and chest radiotherapy. Pooled ECV was 28.44% (95% confidence interval, CI, 26.85-30.03%) among subjects who had undergone cardiotoxic cancer therapy, versus 25.23% (95%CI 23.31-27.14%) among those who had not (p = .003).
A higher ECV in patients who underwent cardiotoxic treatment could imply subclinical changes in the myocardium, present even before overt cardiac pathology is detectable.
The ability to detect subclinical changes in the myocardium displayed by ECV suggests its use as an early biomarker of cancer therapy-related cardiotoxicity.
• Cardiotoxicity is a common adverse effect of cancer therapy; therefore, its prompt detection could improve patient outcomes. • Pooled MRI-derived myocardial extracellular volume was higher in patients who underwent cardiotoxic cancer therapy than in those who did not (28.44% versus 25.23%, p = .003). • MRI-derived myocardial extracellular volume represents a potential early biomarker of cancer therapy cardiotoxicity.
磁共振成像(MRI)衍生的细胞外容积(ECV)可在明显病理学发生之前对心肌变化进行特征描述,而这种变化可能是癌症治疗性心脏毒性导致的。我们的目的是回顾探讨 MRI 衍生的 ECV 作为早期心脏毒性生物标志物以指导及时干预的作用的研究。
2022 年 4 月,我们在 EMBASE 和 PubMed 上进行了系统检索,以查找关于 MRI 衍生的 ECV 作为癌症治疗性心脏毒性生物标志物的文章。两名盲法研究人员筛选了检索到的文章,包括至少在心脏毒性治疗后 3 个月报告 ECV 值的文章。对每篇文章的数据进行提取,包括临床和技术数据以及 ECV 值。使用随机效应模型计算合并的 ECV,并在不同的治疗方案之间以及在出现或未出现明显心功能障碍的患者之间进行比较。进行了荟萃回归分析,以评估哪些临床或技术变量对 ECV 有显著影响。
共纳入 19 项研究。研究人群范围为 9 至 236 例患者,共 1123 人,平均年龄为 12.5 至 74 岁。大多数研究纳入了接受蒽环类药物和胸部放疗的乳腺癌或食管癌患者。接受心脏毒性癌症治疗的患者的 ECV 为 28.44%(95%置信区间,CI,26.85%至 30.03%),而未接受治疗的患者为 25.23%(95%CI,23.31%至 27.14%)(p=0.003)。
接受心脏毒性治疗的患者中 ECV 升高可能意味着心肌存在亚临床变化,甚至在可检测到明显的心脏病理学之前就已经存在。
ECV 显示出检测心肌亚临床变化的能力,提示其可作为癌症治疗相关性心脏毒性的早期生物标志物。
心脏毒性是癌症治疗的常见不良反应;因此,及时检测可改善患者的结局。
接受心脏毒性癌症治疗的患者的 MRI 衍生心肌细胞外容积高于未接受治疗的患者(28.44%比 25.23%,p=0.003)。
MRI 衍生的心肌细胞外容积代表癌症治疗性心脏毒性的潜在早期生物标志物。